Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2023 May 16;15(5):e39096.
doi: 10.7759/cureus.39096. eCollection 2023 May.

A Unique Presentation of a Thoracic Conundrum: Tracheobronchial Rests in the Esophagus

Affiliations
Case Reports

A Unique Presentation of a Thoracic Conundrum: Tracheobronchial Rests in the Esophagus

Abhijith Lakshman et al. Cureus. .

Abstract

Tracheobronchial rests are a rare congenital anomaly where ectopic respiratory tract elements may be found in an abnormal site, such as within the esophageal wall. We present a case of a late presentation of an esophageal intramural tracheobronchial rest with complaints of pain in the left chest wall, vomiting, and loss of appetite for one month. The chest X-ray and mammogram were both normal, but an endoscopy could not be performed due to luminal narrowing. A CT scan shows a well-defined, round, non-enhancing hypodense lesion measuring 2.6 x 2.7 cm in the middle one-third of the esophagus. Upon resection, histopathological examination revealed fragments of tissue lined by pseudostratified ciliated columnar epithelium with respiratory mucinous glands admixed with pools of mucin and underlying strands of skeletal muscle. The subepithelium contains esophageal submucosal glands, which confirm the esophageal origin of the choristoma. The usual presentation is congenital esophageal stenosis at birth with over half of these cases being attributed to tracheobronchial rests. Presentation beyond adolescence is even rarer with a relatively benign course and favorable prognosis. Clinical, radiological, and pathological correlation as well as a high index of suspicion are important to avoid misdiagnosis and to institute optimal treatment.

Keywords: choristoma; congenital; esophageal stenosis; heterotopia; rests; tracheobronchial.

PubMed Disclaimer

Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Figure 1
Figure 1. CT lung (transverse view) showing an esophageal mass (white arrow)
A well-defined, round, non-enhancing hypodense lesion measuring 2.6 x 2.7 cm in the para-esophageal region on the left side from the middle one-third of the esophagus
Figure 2
Figure 2. Non-FDG avid non-enhancing lesion (40 x 27 x 35 mm, SUV max 1.05) seen along the left lateral wall of the distal esophagus (white arrow)
Figure 3
Figure 3. Respiratory epithelium with underlying bundles of skeletal muscle (H&E stain at 400x magnification)
Figure 4
Figure 4. Respiratory epithelium and an adjacent pool of extracellular mucin containing numerous neutrophils and eosinophils (H&E stain at 400x magnification)
Figure 5
Figure 5. Subepithelium of the muscular fragment with an underlying submucosal gland, indicative of an esophageal origin (H&E stain at 400x magnification)

References

    1. An unusual presentation of congenital esophageal stenosis due to tracheobronchial remnants in a newborn prenatally diagnosed with duodenal atresia. Mai C, Breysem L, De Hertogh G, Van Raemdonck D, Smet MH. J Belg Soc Radiol. 2015;99:43–46. - PMC - PubMed
    1. Congenital esophageal stenosis due to tracheobronchial remnants and its associated anomalies. Nishina T, Tsuchida Y, Saito S. J Pediatr Surg. 1981;16:190–193. - PubMed
    1. Congenital oesophageal stenosis caused by tracheobronchial structures in the oesophageal wall. Ibrahim NB, Sandry RJ. Thorax. 1981;36:465–468. - PMC - PubMed
    1. Congenital esophageal stenosis due to tracheobronchial remnants. Ishida M, Tsuchida Y, Saito S, Tsunoda A. https://www.sciencedirect.com/science/article/abs/pii/0022346869906794. J Pediatr Surg. 1969;4:339–345. - PubMed
    1. Congenital esophageal stenosis: a rare malformation of the foregut. Brzački V, Mladenović B, Jeremić L, et al. Nagoya J Med Sci. 2019;81:535–547. - PMC - PubMed

Publication types

LinkOut - more resources